新型吡嗪酮类席夫碱化合物的设计合成及抑菌性能研究
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摘要
Schiff碱是一类非常重要含氮配体,它的-RC=N-双键官能团使其具有易配位、易成环等特点。迄今国内外化学工作者不断开展此领域的工作,合成了各类Schiff碱及其金属配合物,研究和开发了多方面的用途。其中氮杂环Schiff碱配体及其过渡金属配合物的良好生物活性日益引起了人们的注意,因此设计合成这种Schiff碱配体及其过渡金属配合物具有重要的化学与生物学意义。
     本论文首次由2-乙酰基吡嗪为原料设计合成了4种吡嗪酮类Schiff碱配体。实验发现,苯胺对位取代基结构不同与2-乙酰吡嗪发生Schiff碱缩合反应活性也不相同,得到反应活性顺序为:4-甲氧基苯胺>4-甲基苯胺>4-氯苯胺>4-溴苯胺。对4种Schiff碱配体进行了元素分析、核磁共振、红外、紫外光谱等方法表征。实验中对两种制备Schiff碱配体的方法(传统方法和微波方法)进行了对比。4种Schiff碱配体分别与过渡金属Fe()、Co(Ⅱ)、Ni(Ⅱ)、Cu(Ⅱ)合成了16种Schiff碱配合物,并对16种Schiff碱配合物进行了元素分析、红外、紫外光谱等表征。
     本论文着重研究了所得Schiff碱配体和配合物的生物活性。通过对金黄色葡萄球菌、枯草杆菌、大肠杆菌的抑菌活性测试,深入探讨了配体结构、中心金属电子效应与生物活性之间的关系。
     本论文还使用微波技术合成新型Schiff碱配体前躯体3-二甲氨基-1-(2-吡嗪基)-2-丙烯-1-酮。比较了反应过程中常规加热和微波加热对反应的不同影响,发现微波辐射加热条件下的反应时间大为缩短、产率有所提高。应用单因素法,通过系列实验对微波合成方法进行了深入研究,采用响应面优化法对实验条件进行科学可靠性分析,得到最佳实验条件。
Schiff base is a kind of very important N-included ligand,and its functional group of -RC=N-bond is inclined to coordinated with metals and to be tinged formation.Up to the date,all kinds of Sehiff bases and their metal complexes have been synthesized and characterised by researchers,and their application have been exploited in many fields,among which nitrogenous heteroeycle Schiff bases and their metal complexes have been paid more attention due to their special use for bio-activity.Therefore,design and synthesise some new Schiff base ligands and their complexes of transition metals have much signification in chemistry and biology field.
     In this dissertation 2-acetylpyrazine keto Schiff base ligands have been obtained for the first time,and were characterized by elemental analysis,IR,~1HNMR and UV spectra,16 numsers of transition metal(M=Fe(Ⅲ),Co(Ⅱ),Ni(Ⅱ),Cu(Ⅱ)) complexes based on the 2-acetylpyrazine keto Schiff bases have been prepared.The effect factors of the reaction process on aniline-like structure were analyzed in terms of the experiment results,and the result obtain indicates the order of activity as follow:4-methoxyanline>4-methyanline>4-ehloroaniline>4-brom-anilines.The reaction heated by traditional and microwave method was compared in this paper.The emphasis studies are focused on the biology-active of the Sehiff base ligands and their complexes.In the same time,the correlation among electronic property of central metal,the ligand structure and bio-activity are also investigated.
     In this paper,the precursor compounds of anticancer drug 3-dimethylamino-1-(2-pyrazineyl)-2-propylene-1-one has been synthesized by microwave-assisted process.There reaction process by traditional and microwave method was compared to each other respective.Compared with the traditional synthetic method,the same products were obtained with shorter under the microwave radiation with reaction time and in higher yield.The single-factor method and response surface methodology was employed to study the reaction effects,we performed a series of experiments under various reaction time, solvent and power,from which the optimal reaction conditions have been obtained.
引文
[1]Rosenbeig B.,Camp L.V.,Trosko J.E.,et al.Platinum compounds a nuw class of potent anititumourouragents[J].Nature,1969,222:385-386
    [2]杨高文,夏小平,涂欢等.Schiff碱、咪唑金属配合物合成及抗癌活性的荧光筛选研究[J].北学研究与应用,1995,7(1):41-45
    [3]Praveen K.,Sharma,Handa R.N.Synthesis and characterization of some transition metal complexes of N-(2-hydroxy-1-naPhthylidene) amino acids.synth.react[J].Inorg Met Org Chem,1996,26(7):1219-1230
    [4]Angoso A.,Martin-Llorente J.M.,Manzano J.L.Preparation and study of amino acid (DL-leucine,L-isoleucine,L-histidine) sehiff bases with ethyl-o-ketoey-clopentyl carboxylate and the corresponding Copper(Ⅱ)Complexes[J].Inorganic Chimica Acta,1992,195(1):45-49
    [5]王积涛,许育明,杨晓萍等.含氨基酸Schiff碱-金属手性配合物的合成及其相关反应的进展[J].有机化学,1995,15:449-460
    [6]Parmar V.S.,Singh A.,Kirpal S.B.Schiff base of amino acid esters as new substrates for the enantioselective enzymatic hydrolysis and accompanied asymmetric transformations in aqueous organic solvents[J].J Org Chem.,1996,61:1223-1227
    [7]Khoo L.E.,Charland J.P.,Gabe E.J.Synthesis and structural studies for a series of aromatic schiff bases complexes with triphenyltin chloride and triphenyltin isothiocyanate[J].Inorganica Chimina Aeta,1987,128:139-145
    [8]Schiff H.The synthesis and characterization of schiff base[J].Ann.Suppl,,1984,(3):343-349
    [9]王积涛,胡青眉,张宝申等.有机化学[M].南京:南开大学出版社.1993:346-347
    [10]Naeimi H.,Safari J.,Heidamezhad A.Synthesis of schiff base ligands derived from condensation of salicylaldehyde derivatives and synthetic diamine[J].Dyes and Pigments,2007,73:251-253
    [10]West B.O.The magnetic moments and structures of some N-substituted salicylideneimine complexes of cobalt(Ⅱ)[J].J Chem Soc.,1962:1374-1387
    [11]Michael G.,Drew B.,Forida S.,et al.Trihapto-hexahapto fluxional behavior of a macrocyclic ligand:template synthesis,proton nuclear magnetic resonance spectra,and the crystal and molecular structure of an eleven-coordinate barium(Ⅱ) complex[J].J Chem Soc.,1983:1653-1659
    [12]张帆.无机分析用新有机试剂的合成[M].北京:海洋出版社,1992:203-222
    [13]孙宏建,李晓燕,崔学桂等.过渡金属Schiff碱配合物的研究(Ⅱ)-N-水杨醛甘氨酸三毗陡合镍(Ⅱ)热分解非等温动力学的研究[J].高等学校化学学报,1992,13(9):1168-1170
    [14]史卫良,陈德余,陈士明等.水杨醛天冬氨酸过渡金属配合物的ESR波谱及抗O~(2-)-性能[J].无机化学学报,2001,17(2):239-43
    [15]梁芳珍,李晓明.水杨醛双酞胺Cu(Ⅱ)配合物的合成,表征与抑菌活性[J].化学通报,1999,(8):37-39
    [16]Rosenberg B.,Van C.L.The Successful regression of large solid sarcoma 180 tumors by platinum compounds[J].Cancer Res.,1970,30:1799-1802
    [17]Csaszar J.,Morvay J.,Herczeg O.Study of 5-nitro-2-furfuraldehyde derivatives.Ⅱ.preparation,spectra and antibacterial activities of schiff bases with sulfonamides[J].Acta.Phys.Chem.,1985,31(3):711-722
    [18]祝心德,乐芝凤,吴自慎.2,4-二羟基苯甲醛缩氨基硫脲合铜(Ⅱ),镍(Ⅱ),锌(Ⅱ),铁(Ⅱ)的合成和表征及杀菌活性[J].高等学校化学学报,1991,12(8):1066-1068
    [19]Chandra S.,Sharma K.Synthesis and characterization of chrominum(Ⅲ) complex of semicarbazones and thiosemicarbazones[J].Syn.React.Inorg.Met-Org.Chem.,1982,12(6):647-659
    [20]Dutt N.K.,Nag K.Bis-salicylaldehyde ethylenediamine and bis-salicylaldehyde o-phen-ylenedimine complexes of rare-earth[J].Inorg.Nucl.Chem.,1968,30:2493-2499
    [21]Xiucen Y.,Harry G.Evidence for Schiff base in the addition of amino alcohols to the Eu(Ⅲ) chelates of benzoylacetone and dibenzoyl-methanev[J].Inorg.Chim.Acta.,1982,59(2):261-268
    [22]Iftikhar K.,Arvind M.,Ahnad N.Studies on bis(p-dimethylaminobenzylidene) benzidine complexes of Trivalent Lanthanides[J].Indian.J.Chem.,1986,25A:589-591
    [23]李志良,陈建华,章开诚等.席夫碱非铂抗癌络合物初步筛选的荧光法研究[J].中国科学(B辑),1991,11:1193
    [25]Adams H.,Bailey H.A.,Fenton D.E.,et al.Dinuclear copper(Ⅰ) and -(Ⅱ) complexes derived from a ciprotonated schiff base cryptand[J].J.Chem.Soc.,DaltonTrans., 1997:921-925
    [26]Yang X.P.,Jones R.A.,Wong W.K.,et al.Design and synthesis of a near infra-red luminescent hexanuclear Zn-Nd prism[J].Chem.Commun.,2006:1836-1838
    [27]Ferbinteanu M.,Miyasaka H.,Wernsdorfer W.,et al.Single-chain magnet(NEt_4)[Mn_2(5-MeOsalen)_2Fe(CN)_6]made of MnⅢ-FeⅢ-MnⅢ trinuclear single-molecule magnet with an ST=9/2 spin ground state[J].J.Am.Chem.Soc.,2005,127(9):3090-3099
    [28]游效曾,孟庆金,韩万书.配位化学进展[M].北京:高等教育出版社,2000:20
    [29]Hughes R.P.,Linder D.C.,Rheingold A.L.,et al.Synthesis and structure of the thallium(Ⅰ) salt of the tetrakis{3,5-bis(trifluoromethyl)phenyl}borate anion[J].Inorg Chem,1997,36(8):1726-1727
    [30]李培凡,刘燕,王智等.配合物的合成、结构和Cu(Ⅱ)配合物的抑菌活性[J].天津师范大学学报(自然科学版),2003,23(4):13-15
    [31]孙宏建,李晓燕,崔学桂等.过渡金属Schiff碱配合物研究[J].高等学校化学学报,1992,13(9):1168-1170
    [32]张淑华.5-溴,N(2-磺酸基乙基)水杨醛亚胺Schiff碱的合成及表征[J].化工技术与开发,2003,32(2):14-15
    [33]张淑华.5-硝基,N(2-磺酸基乙基)水杨醛亚胺Schiff碱的合成、表征及抑菌活性[J].广西科学,2003,10(4):284-285
    [34]蒋毅民,张淑华,许庆等.双核Cu(Ⅱ)-牛磺酸缩水杨醛Schiff碱配合物的合成、晶体结构及生物活性[J].化学学报,2003,61(4):578
    [35]李桂芝.2种水杨醛缩氨基酸及其种金属配合物的杀菌活性研究[J].聊城大学学报(自然科学版),2003,15(1):57-59
    [36]Abdel-Latif S.A.,Hassib H.B.,Issa Y.M.Studies on some salicylaldehyde schiff base derivatives and their complexes with Cr(Ⅲ),Mn(Ⅱ),Fe(Ⅲ),Ni(Ⅱ)andCu(Ⅱ)[J].Spectrochimica Acta Part A.2006
    [37]赵文岩,牛雪平,张蕊.新型水杨醛2芳胺席夫碱化合物的合成及生物活性[J].中国药学,2005,40(1):63-66
    [38]赵继全,韩建萍,张月成.丙氨酸-水杨醛席夫碱锰(Ⅲ)配合物的制备及其对烯烃环氧化的催化性能[J].催化学报,2005,26(7):571-576
    [39]李茂莲.几种水杨醛氨基酸Schiff碱的合成及性质研究[J].化学世界,2008, 49(5):317-318
    [40]Hodnett E.M.,Dunn W.J.Structure-antitumor activity correlation of some Schiff bases[J].Journal of medicinal chemidtry,1970,13(4):768-770
    [41]Hodnett E.M.,Mooney P.D.,Anititumor activities of some Sehiff bases[J].Journal of medicinal chemidtry,1970,13(4):786
    [42]朱传方,吴爱斌,徐汉红.2,4-二羟基苯乙酮席夫碱化合物的合成[J].化学试剂,2001,23(3):150-151
    [43]刘建宁,张兵,徐博万等.2,4-二羟基苯乙酮腙类试剂的合成[J].化学试剂,2002,24(5):294-295
    [44]张兵,刘建宁,仵博万,于新桥,赵建社.2,4-二羟基苯乙酮双席夫碱化合物的合成[J].化学试剂,2003,25(6):355-356
    [45]张兵,仵博万,于新桥,刘建宁.2,4-二羟基苯乙酮席夫碱化合物的合成与表征[J].陇东学院学报(自然科学版),2005,15(1):40-42
    [46]姚克敏,吴大庆,杨卫红.苯甲酰丙酮缩乙二胺与镧系元素多核配合物的合成与表征[J].应用化学,1992,9(4):8-12
    [47]李锦洲,沙靖全,安郁美等.呋喃甲酰基吡唑啉酮所氨基硫脲稀土配合物的合成、表征及生物活性[J].中国稀土学报,2002,20(23):56-58
    [48]李锦洲,李刚,于文锦.呋喃甲酰基吡唑啉酮双席夫碱稀土配合物的合成、表征及生物活性[J].中国稀土学报,2000:18(1):71-73
    [49]李锦洲,于文锦,李刚.噻吩甲酰基吡唑啉酮缩乙二胺稀土配合物的合成、表征及生物活性[J].应用化学,2000:17(3):280-282
    [50]高健,相海鹰,许同桃等.丹皮酚及其席夫碱衍生物的抑菌性研究[J].化学试剂,2007,29(1):59-60;62
    [51]钟霞.新型酮类Schiff碱金属配合物的研究[D].兰州:兰州大学博士学位论文
    [52]Vigato P.A.,Fenton D.E.Shift base complexes of lanthanides and actinides[J].Inorg Chim Acta,1987,139:39-48
    [53]Cupta A.K.,Bhargava K.P.,Pharmazie,same trlazole anaglogs as anti inflammatory agents[J].1978,33(1):430-431
    [54]Kamigaito M.,Ando T.,Sawamoto M.Metal-catalyzed living radical polymerization[J].Chem.Rev.,2001,101(12):3689-3746
    [55]Mohan M.,Kumar M.,Kumar A.,et al.Synthesis,charoterization and antitumor activity of iron(Ⅱ) and iron(Ⅲ) complexes of N-heterocyclic carboxaldehyde thiosemicarbazones[J].J Inorg Biochem.,1988,32:239
    [56]Lu X.H.~a,Xia Q.H.~(a,*),Zhan H.J.~(a,b),et al.Synthesis,characterization and catalytic property of tetradentate Schiff-base complexes for the epoxidation of styrene[J].Journal of Molecular Catalysis A:Chemieal,2006,250:62-69
    [57]孟庆金,王瑞雪,步修仁.新的不对称双Schiff碱镍配合物[J].高等学校化学学报,1990,11(10):1126-1128
    [58]Gedye R.,Smith E,Westaway K.,et al.The use of microwave ovens for rapid organic synthesis[J].Tetrahedron Lett,1986,27(3):279-284
    [59]金钦汉,戴树珊,黄卡玛.微波化学[M].(2).科学出版社,2001:5
    [60]Nikolai K.,Timothy N.D.Highly diastereoseleetive synthesis of 1,3-oxazolidines under thermodynamic control using focused microwave irradiation under solvent-free conditions[J].Green Chem.,2001,3:6
    [61]Vasudevan V.N.,Rajender S.V.Microwave-aceelerated suzuki cross-coupling reaction in Polyethylene glycol(PEG)[J].Green Chem.,2001,3:146-148
    [62]Goverdhan L.K.,Monica B.,Jasamrit K.,ea al.Solbentless preparation of oximes in the solid state and via microwave irradiation[J].Gree Chem.,2001,3:275-277
    [63]Tetsushi Y.,Yuji W.,Hirotaka E.,et.al.Microwave-assisted solvent-free instantaneous claisen rearrangement for synthesis of bis(3-allyl-4-hydroxyphenyl) sulfone[J].Green Chem.,2003,5:690-692
    [64]Rmesh C.,Mahender G.,Ravindranath N.,et al.A convenient,rapid,highly selective and eco-friendly supported ammonium formate under microwave irradiation[J].Green Chem.,2003,5:68-70
    [65]Ronald T.,Matthias N.,Bernd O.Microwave assisted phosgenation alcoholysis using triphosgene[J].Green Chem.,2003,5:285-290
    [66]Peng Y.Q.,Song G.H.Combined microwave and ultrasound accelerated Knoevenagel-Doebner reaetion in aqueous media:agreen route to 3-aryl acrylic acids[J].Green Chem.,2003,5:704-706
    [67]Bai L.,Wang J.X.,Zhang Y.M.Rapid microwave-promoted suzuki cross coupling reaction in water[J].Green Chem.,2003,5:615-617
    [68]Janine F.,Matthias N.,Bernd O.Oxidation of styrene and cyclohexene under microwave conditions[J].Green Chem.,2003,5:291-295
    [69]Nuehter M.,Ondrusechka B.,Bonrath W.,et al.Microwave assisted synthesis-a critical technology overview[J]:Green Chem.,2004,6:128-141
    [70]Vanya B.K.,Carlos A.M.A.Solvent -free synthesis of melamines under microwave irradiation[J].Green Chem.,2004,6:183-187
    [71]Nieholas E.,Leadbeater M.M.Rapid and amenable suzuki coupling reaction in water using microwave and conveniional heating[J].J.Org.Chem.,2003,68:885-892
    [72]Bogdal D.,Lukasiewiez M.,Pielichowski J.Halogenation of carbazole and other aromatic compounds with hydrohalic acids and hydrogen peroxide under microwave irradiation[J].Green Chem.,2004,6:110-113
    [73]Nabajyoti D.,Anne M.,Ahcene B.Microwave mediated solvent-free acetylation of deactivated and hidered phenols[J].GreenChem.,2001,3(5):263-264
    [74]Lidstr(O|¨)m P.,Tierney J.,Wathey B.,et al.Microwave assisted organic synthesis-a review[J].Tetrahedron,2001,57:9225-9283
    [75]Villemin D.,Benalloum A.,Dry reaction under microwave:condensation of sulfones with aldehydes on KF-Alumina[J].Synth.Commun.,1991,21(1):63-68
    [76]Bose A.K.,Manhas M.S.,Chosh M.,et al.Highly accelerated reactions in a microwave oven:syhthesis of heterocycles[J].Heterocycles,1990,30(3):741-747
    [77]Liu F.,Li Y.,Xu W.G.The use of microwave irradiation for the rapid oranic synthesis[J].Chem.Res.Chin.Univ.,1993,(2):168-170
    [78]李耀先,刘在群,徐文国等.微波常压合成缩醛(酮)[J].吉林大学自然科学学报,1996,8(3):72-74
    [79]张恭孝,杨荣华.席夫碱金属配合物的研究进展[J].山东化工,2004,33:14-17
    [80]郑允飞,陈文纳,李德昌等.Schiff碱及其配合物的应用研究进展[J].化工技术与开发,2004,33(4):26-29
    [81]杨高文,夏小平,涂欢等.Schiff碱、咪唑金属配合物合成及抗癌活性的荧光筛选研究[J].化学研究与应用,1995,7(1):41-45
    [82]Opozda E.M.~(a,*),Wieslaw L.~b,Barbara W.G.~b Synthesis and characterisation of unsymmetrical Schiff bases derived from 3,4-diaminopyridine.Crystal and molecular structure of hydrogen-bonded dimers of 3-{[(4-aminopyridin-3-yl)amino]methylene}pentane-2,4-dione[J].Journal of Molecular Structure,2006(784):149-156
    [83]王积涛,许育明,杨小萍等.含氨基酸Schiff碱-金属手性配合物的合成及其相关反应进展[J].有机化学,1995,15:449-460
    [84]夏江滨,杨红,李富友等.新型席夫碱锌配合物的合成及其在染料敏化太阳能电池中的应用[J].高等学校化学学报,2006,27(2):204-207
    [85]Baker A.W.,Shulgin A.T.Intramolecular hydrogen bonding.Ⅱ.the determination of hammer sigma constants by intramolecular hydrogen bonding in Schiffs Bases[J].J.Am.Chem.Soc.,1959,81(7):1523-1529
    [86]游效曾,孟庆金,韩万书主编.配位化学进展[M].北京:高等教育出版社,2000,17-27
    [87]李君,张逢星,唐宗薰等.Mn(Ⅲ)Schiff碱配合物的合成结构及性能表征[J].无机化学学报,2000,16(1):84-88
    [88]刘树祥,刘春丽,田来进等.锌(Ⅱ)氨基酸水杨醛席夫碱-α-氨基酸三元配合物的稳定性[J].无机化学学报,1999,15(1):114-117
    [89]张存根,冷拥军,顾建明.Schiff碱与锰(Ⅲ)的单核和双核配合物的合成及结构[J].无机化学学报,1999,15(5):583-589
    [90]柳翠英,郭秀英.5-硝基,N(2-羟基乙基)水杨醛亚胺Schiff碱的合成[J].化学试剂,1994,16(6):368-369
    [91]梁芳针,徐克花,任建成.2-氨基噻唑缩取代水杨醛Zn(Ⅱ)配合物的合成、表征及抑菌活性[J].合成化学,1999,7(2):121-124
    [92]Kalinowski D.,Sharpe P.C.,Bernhardt P.V.,et al.Structure-activity relationships of novel iron chelators for thetreatment of iron overload disease:The methyl pyrazinylketoneisonicotinoyl hydrazone series[J].J.Med.Chem.2007,51(2):331-344
    [93]Opletalova V.,Kalinowski D.S.,Vejsova M.,et al.Identification and characterization of thiosemicarbazones with antifungal and antitumor effects:cellular iron chelation mediating cytotoxic activity[J].Chem.Res.Toxicol.,2008,21(9):1878-1889
    [94]Kalinowski D.S.,Sharpe P.C.,Bernhardt P.V.,et al.Design,synthesis and characterization of new iron chelators with anti-proliferative activity:Structure-activity relation-ships of novel thiohydrazone analogs[J].J.Med.Chem.2007,50(24):6212-6225
    [95]Yatsmilski K.B.,translated by YU Xun(余绚),WU Yao-M an(吴瑶曼)Elementary Bio-Inorganic Chemistry(生物无机化学入门)[M],Beijing:Science Press,1984:116
    [96]Opletalova V.,Kalinowski D.S.,Vejsova M.,et al.Identification and characterization of thiosemicarbazones with antifungal and antitumor effects:cellular iron chelation mediating cytotoxic activity[J].Chem.Res.Toxicol.,2008,21(9):1878-1889
    [97]Kalinowski D.S.,Sharpe P.C.,Bernhardt P.V.,et al.Structure-Activity Relationships of Novel Iron Chelatorsfor the Treatment of Iron Overload Disease:The MethylPyrazinylketone Isonicotinoyl Hydrazone Series[J].J.Med.Chem.,2008,51(2):331-344
    [98]Kushner S.,Dalalian H.,Sanjurjo J.L.,et al.Experimental Chemotherapy of Tuberculosis.Ⅱ.TheSynthesis of Pyrazinamides and Related Compounds[J].J.Am.Chem.Soc.,1952,74(14):3617-3621
    [99]Siriwardana A.I.,Kathriarachchi K.K.A.D.S.,Nakamura I.,et al.Synthesis of pyddinylpyrrole derivatives via the palladium-catalyzed reaction of acetylpyridines with methyleneaziridines[J].J.Am.Chem.Soc.,2004,126(43):13898-13899
    [100]Christian R.K.,Roland B.,Eichinger R.,et al.Gallium(Ⅲ) and Iron(Ⅲ) complexes of α-N-Heterocyclic thiosemicarbazones:synthesis,characterization,cytotoxicity,and interaction with ribonucleotide reductase[J].J.Med.Chem.,2007,50(6):1254-1265
    [101]Papaefstathiou G.S.,Perlepes S.P.Families of polynuclear manganese,cobalt,nickel and copper complexes stabilized by various forms of di-2-pyridyl ketone[J].Inorg.Chem.,2002,23(4):249-274
    [102]Tummler B.,Maass G.,Wber E.,et al.Noncycic crown-type polyethers,pyridinophane crytands,and their alkali metal ion complexes:synthesis,complex stability,and kinetics[J].J.Am.Chem.Soc.,1977,99(14):4683-4690
    [103]Koutsidis G.,Fuente A.D.,Dimitriou C.,et al.Acrylamide and pyrazine formation in model systems containing asparagine[J].J.Agric.Food Chem.,2008,56(15):6105-6112
    [104]Zhao W.,Song Y.,Okamura T.,et al.Syntheses,crystal structures,and magnetic properties of novel manganese(Ⅲ) complexes with flexible tripodal ligand 1,3,5-tris(imidazol-1-ylmethyl)-2,4,6-trimethylbenzene[J].Inorg.Chem.,2005,44(9):3330-3336
    [105]Chien C.H.,Chang J.C.,Yeh C.Y.,et al.Weak antiferromagnetic coupling for novel linear hexanuclear nickel(Ⅱ) string complexes[J].Dalton Trans.,2006:3249-3256
    [106]Nakedia M.F.,Carvalho,Adolfo H.Jr.,et al.Synthesis and characterization of three mononuclear Fe(Ⅲ) complexes containing bipodal and tripodal ligands:X-ray molecular structure of the dichloro[N-propanamide-N,N-bis-(2-pyridylmethyl)amine]iron(Ⅲ)perchlorate[J].Inorg.Chim.Acta,2006,359:90-99
    [107]Houminer Y.,Southwick E.W.,Williams D.L.Substituent-directing effects in the homolytic acylation of pyrazine derivatives[J].J.Org.Chem.,1989,54(3):640-643
    [108]Fan W.L.,Xu Y.,Zhang Y.H.Characterization of pyrazines in some Chinese liquors and their approximate concentrations[J].J.Agric.Food Chem.,2007,55(24):9956-9962
    [109]Houminer Y.,Southwick,E.W.et al.Substituent-directing effects in the homolytic acylation of pyrazine derivatives[J].J.Org.Chem.,1989,54(3):640-643
    [110]Klumpp D.A.,Garza M.,Sanchez G.V.,et al.Electrophilic activation of acetyl-substituted heteroaromatic compounds[J].J.Org.Chem.,2000,65(26):8997-9000
    [111]Jia W.L.,Song D.T.,Wang S.N.Blue luminescent three-coordinate organoboron compouds with a 2,2'-dipyridylamino functional group[J].J.Org.Chem.,2003,68(3):701-705
    [112]Gerald W.A.,Davis M.C.,Martin A.R.,et al.Antimycobacterial activity of substituted isosteres of pyridine and pyrazinecarboxylic acids[J].J.Med.Chem.,1998,41(13):2436-2438
    [113]Gerald A.W.,Matt C.D.,Arnold R.M.,et al.Antimycobacterial activity of substituted isosteresof pyridine and pyrazinecarboxylic acids[J].J.Med.Chem.,1998,41(13):2436-2438
    [114]黄小凤,李晓林,李中林.杂环类香料的现状与展望[J].化学通报,1995,(8):1-16
    [115]金钦汉,戴树珊,黄卡玛.微波化学[M].北京:科学出版社,1999:1
    [116]Gedye R.,Smith F.,Westaway K.,et al.The use of microwave ovens for rapid organic sythesis[J].Tetrahedron Lett.,1986,27(3):279-282
    [117]张兵,刘建宁,仵博万等.2,4-二羟基苯乙酮双席夫碱化合物的合成[J].化学试剂,2003,25(6):355-356
    [118]张兵,仵博万,于新桥等.2,4-二羟基苯乙酮席夫碱化合物的合成与表征[J].陇东学院学报(自然科学版),2005,15(1):40-42
    [119]吴惠君,陈良,杨俐萍.有机化学[M].上海:华东师范大学出版社,1996:303
    [120]Hossein N.~*,Khadigeh R.,Fariba Salimi,Rapid,efficient and facile synthesis and characterization of novel Schiff bases and their complexes with transition metal ions,Dyes and Pigments 2006:1-4
    [121]尹汉东,马春林,王大奇.吡啶基羧酸苄基锡配合物的红外光谱[J].分析测试学报,1999,18(6):47-49
    [122]Kaafarani,B.R.,Wex,B.,Wang,F.,et al.Synthesis of highly fluorescently yenyne dendri-mers with four and six arms[J].J.Org.Chem,2003,68(13):5377-5380
    [123]Darriet J.,Haddad M.S.,Duesler E.N.,et al.Crystal strueture and magnetic properties of bis(pyrazine)eopper(Ⅱ)perchlorate,Cu(pyz)_2(ClO_4)_2,a two-dimensional Heisenberg antiferromagnet[J],Inorg.Chem,1979,18:2679-2682
    [124]Naeimi H.,Rabiei K.,Salimi F.Rapid,efficient and facile synthesis and characterization of novel Schiff bases and their complexes with transition metal ions[J],Dyes and Pigments,2006:1-4
    [125]Wchter G A.,Davis M.C.,Martin A.R.,et al.Antimycobacterial activity of substituted isosteres of pyridine and pyrazinecarboxylic acids[J].J.Med.Chem.,1998,41(13):2436-2438
    [126]Koutsidis G.,Fuente A.D.,Dimitriou C.,et al.Acrylamide and pyrazine formation in model systems containing asparagine[J].Agric.Food Chem.,2008,56(15):6105-6112
    [127]于文锦,李锦州,李刚.唆吩甲酸毗哇琳酮缩乙二胺配合物的合成、表征及生物活性[J].无机化学学报,1999,15(5):657-660
    [128]Zitouni T.,G(?)(?)ldhan,Kaplanc(?)(?)kl(?)(?),Zafer As(?)(?)m,et al.Synthesis and antimicrobial activity of 4-phenyl/cyclo hexyl-5-(1-phenoxyrthyl)-3-[N-(2-thiazolyi)-acetamido]thio-4H-1,2,4-triazole derivatives[J].European Journal of Medicinal Chemistry,2005,40(6):607-613
    [129]Kim D.K.,Kim J.,Park H.J.Design,synthesis,and biological evaluation of novel 2-pyridinyl-[1,2,4]triazoles as inhibitors of transforming growth factor β1 type 1 receptor[J].Bioorganic and Medicinal Chemistry,2004,12(9):2013-2020
    [130]Kalinowski D.S.,Richardson D.R.The evolution of iron chelators for the treatment of iron overload disease and cancer[J].Pharmacol,2005,57:547-583
    [131]Easmon J.,Heinisch G.,Holzer W.,et al.Novel thiosemicarbazones derived from formyi-and acyldiazines:Synthesis,effect on cell proliferation,and synergism with antiviral agents[J].J.Med.Chem,1992,35:3288-3296
    [132]范秀容,李广武,沈萍.微生物学实验[M].北京:高等教育出版社, 1989:16-21;99-103
    [133]Chien J.H.,Tang J.L.,et al.Detection of BCR-ABL gene mutations in Philadelphia chromosome positive leukemia patients resistant to STI-571 cancer therapy[J].Leukemia Research,2008,32:1724-1734
    [134]金钦汗.微波化学[M].北京:科学出版社,1999:2
    [135]Faravelli L.A response surface approach for reliability analysis[J].Journal of Engineering Mechanics,1989,115(12):2763-2781
    [136]刘毅锋,张娟,DMF二烷基缩醛及其衍生物的合成[J].西北大学学报(自然科学版),1996,26(3):240-242
    [137]白亚军,刘毅锋等.3-N,N-二甲基氨基-1-芳杂环基-2-丙稀-1-酮合成[J].西北大学学报(自然科学版),2006,37(2):231-234